CDK9-mediated transcription elongation is required for MYC addiction in hepatocellular carcinoma

Abstract

By screening a custom library of shRNAs directed toward known drug targets in a genetically defined Myc-driven hepatocellular carcinoma model, Huang et al. identified Cdk9 as required for disease maintenance. Pharmacological or shRNA-mediated CDK9 inhibition led to robust anti-tumor effects that correlated with MYC expression levels and depended on the role that both CDK9 and MYC exert in transcription elongation. This study proposes CDK9 inhibition as a therapeutic strategy for MYC-overexpressing liver tumors and highlights the relevance of transcription elongation in the addiction of cancer cells to MYC.

Abstract

One-year survival rates for newly diagnosed hepatocellular carcinoma (HCC) are <50%, and unresectable HCC carries a dismal prognosis owing to its aggressiveness and the undruggable nature of its main genetic drivers. By screening a custom library of shRNAs directed toward known drug targets in a genetically defined Myc-driven HCC model, we identified cyclin-dependent kinase 9 (Cdk9) as required for disease maintenance. Pharmacological or shRNA-mediated CDK9 inhibition led to robust anti-tumor effects that correlated with MYC expression levels and depended on the role that both CDK9 and MYC exert in transcription elongation. Our results establish CDK9 inhibition as a therapeutic strategy for MYC-overexpressing liver tumors and highlight the relevance of transcription elongation in the addiction of cancer cells to MYC.